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P4‐193: Presenilin 2 and the gamma‐secretase complex in microglia function
Author(s) -
Jayadev Suman,
Case Amanda,
Nguyen Huy,
Seaburg Luke,
Garden Gwenn A.
Publication year - 2008
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2008.05.2260
Subject(s) - microglia , neuroinflammation , neurodegeneration , amyloid precursor protein , microbiology and biotechnology , presenilin , inflammation , biology , amyloid precursor protein secretase , chemistry , alzheimer's disease , immunology , medicine , disease
and G384A were subjected to treatment with different GSMs, and A 42 and A 38 levels were analyzed by ELISA, mass spectrometry or high-resolution SDS-urea electrophoresis. Results: After sulindac sulfide treatment, all mutant cell lines displayed a strongly reduced A 42response as compared to WT-PS1 expressing cells. Conversely, A 38 levels were increased to similar levels in the mutant cell lines. These results were confirmed with the structurally divergent GSM ibuprofen. Furthermore, mass spectrometry and SDS-urea electrophoresis did not reveal compensatory changes in levels of other secreted or intracellular A peptides. Conclusions: These data provide evidence that A 42 and A 38 can be generated independently by -secretase, and argue against a precursor-product relationship between these peptides.